Senior Clinical Research Coordinator

At least two years of experience managing multiple phase 2-4 industry-sponsored clinical trial studies as the primary coordinator required

Strong understanding of FDA regulations, ICH-GCP, and clinical trial operations

Experience with EDC, IVRS, and clinical research platforms

Proficiency in medical terminology and clinical documentation

Provide the highest level of care for study patients

Deliver excellent customer service to pharmaceutical clients

Coordinate all aspects of assigned clinical trials from site initiation through close-out

Maintain compliance with protocols, GCP/ICH guidelines, FDA regulations, IRB requirements, and SOPs

Manage subject recruitment, informed consent, and retention activities

Ensure timely EDC data entry and resolution of queries

Artemis Institute for Clinical Research in Riverside is a patient-centered clinical research site and part of the Headlands Research family. Founded with a core mission to

prioritize patients, advance medicine, and improve the world

, Artemis combines rigorous, process-driven trial management with a compassionate approach to care. The site conducts high-quality clinical trials across multiple therapeutic areas—including psychiatric, metabolic, vaccine, and healthy volunteer studies—and has helped thousands of participants contribute to meaningful medical advancements. Artemis is known for its collaborative team culture, strong operational standards, and commitment to excellence in delivering reliable, protocol-compliant research on behalf of pharmaceutical and biotech sponsors.